Fluoropyrimidine-induced toxicity and DPD deficiency.. A case report of early onset, lethal capecitabine-induced toxicity and mini review of the literature. Uridine triacetate: Efficacy and safety as an antidote. Is it accessible outside USA?


Journal

Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372

Informations de publication

Date de publication:
Apr 2020
Historique:
pubmed: 7 8 2019
medline: 2 9 2020
entrez: 7 8 2019
Statut: ppublish

Résumé

Fluoropyrimidine-based regimens are among the most commonly used chemotherapy combinations for the treatment of solid tumors. Several genetic polymorphisms that are implicated with fluoropyrimidine anabolism and catabolism have been associated with the development of life-threatening toxicities. Uridine triacetate is an FDA-approved antidote for 5-fluorouracil or capecitabine overdose and early-onset, life-threatening toxicity within 96 h of last chemotherapy dose. To date, it is not accessible for Greek patients as per the current summary of product characteristic's time restrictions. We report and discuss the course and outcome of capecitabine toxicity in a 66-year-old female colorectal cancer patient with heterozygous dihydropyrimidine dehydrogenase deficiency. This paper highlights the difficulty in timely access of this lifesaving medication for Greek and possibly other European patients.

Identifiants

pubmed: 31382864
doi: 10.1177/1078155219865597
doi:

Substances chimiques

Acetates 0
Antidotes 0
Antimetabolites, Antineoplastic 0
uridine triacetate 2WP61F175M
Capecitabine 6804DJ8Z9U
Uridine WHI7HQ7H85

Types de publication

Case Reports Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

747-753

Auteurs

Dimitra Ioanna Lampropoulou (DI)

Second Department of Medical Oncology, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

Konstantinos Laschos (K)

Second Department of Medical Oncology, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

Anna-Lea Amylidi (AL)

Second Department of Medical Oncology, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

Ariadni Angelaki (A)

Second Department of Medical Oncology, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

Nikolaos Soupos (N)

Second Department of Medical Oncology, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

Sotirios Boumpoucheropoulos (S)

Second Department of Medical Oncology, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

Eirini Papadopoulou (E)

GeneKor Medical SA, Athens, Greece.

Evgenia Nanou (E)

Faculty of Nursing, Kapodistrian University of Athens, Athens, Greece.
Intensive Care Unit, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

Vasilios Zidianakis (V)

Faculty of Nursing, Kapodistrian University of Athens, Athens, Greece.
Intensive Care Unit, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

George Nasioulas (G)

GeneKor Medical SA, Athens, Greece.

George Fildissis (G)

Faculty of Nursing, Kapodistrian University of Athens, Athens, Greece.
Intensive Care Unit, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

Gerasimos Aravantinos (G)

Second Department of Medical Oncology, General Oncology Hospital of Kifissia "Agioi Anargiroi", Athens, Greece.

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Classifications MeSH